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Vol. 11, Issue 5, 710-730, May 2001

LETTER
From First Base: The Sequence of the Tip of the X Chromosome of Drosophila melanogaster, a Comparison of Two Sequencing Strategies

Panayiotis V. Benos,1,15 Melanie K. Gatt,2,11 Lee Murphy,3 David Harris,3 Bart Barrell,3 Concepcion Ferraz,4 Sophie Vidal,4 Christine Brun,4 Jacques Demaille,4 Edouard Cadieu,5 Stephane Dreano,5 Stéphanie Gloux,5 Valerie Lelaure,5 Stephanie Mottier,5 Francis Galibert,5 Dana Borkova,6 Belen Miñana,6 Fotis C. Kafatos,6 Slava Bolshakov,6,7 Inga Sidén-Kiamos,7 George Papagiannakis,7 Lefteris Spanos,7 Christos Louis,7,8 Encarnación Madueño,9 Beatriz de Pablos,9 Juan Modolell,9 Annette Peter,10 Petra Schöttler,10 Meike Werner,10 Fotini Mourkioti,10 Nicole Beinert,10 Gordon Dowe,10 Ulrich Schäfer,10 Herbert Jäckle,10 Alain Bucheton,4 Debbie Callister,11 Lorna Campbell,11 Nadine S. Henderson,11 Paul J. McMillan,11 Cathy Salles,11 Evelyn Tait,11 Phillipe Valenti,11 Robert D.C. Saunders,11,12 Alain Billaud,13 Lior Pachter,14 David M. Glover,2,11 and Michael Ashburner1,2,16

1 EMBL Outstation, The European Bioinformatics Institute, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SD, UK; 2 Department of Genetics, University of Cambridge, Cambridge, CB2 3EH, UK; 3 Sanger Centre, Wellcome Trust Genome Campus, Hinxton, Cambridge, CB10 1SA, UK; 4 Montpellier University Medical School, IGH-Institut de Génétique Humaine-CNRS, 34396 Montpellier Cedex 5, France; 5 UPR 41, CNRS, Recombinaisons Génétiques, Faculte de Medecine, 35043 Rennes Cedex, France; 6 European Molecular Biology Laboratory (EMBL), D-69117 Heidelberg, Germany; 7 Institute of Molecular Biology and Biotechnology, FORTH, GR-71110 Heraklion, Greece; 8 Department of Biology, University of Crete, 71409 Heraklion, Crete, Greece; 9 Centro de Biología Molecular Severo Ochoa, CSIC and Universidad Autónoma de Madrid, 28049 Madrid, Spain; 10 Max-Planck-Institut für biophysikalische Chemie, Department of Molecular Developmental Biology, D-37070 Göttingen, Germany; 11 Department of Anatomy and Physiology, CRC Cell Cycle Genetics Group, University of Dundee, Dundee, DD1 4HN, UK; 12 Department of Biological Sciences, The Open University, Milton Keynes, MK7 6AA, UK; 13 Fondation Jean Dausset-CEPH (Centre d'Etude du Polymorphisme Humain), 75010 Paris, France; 14 Department of Mathematics, University of California at Berkeley, California 94720-3840, USA

We present the sequence of a contiguous 2.63 Mb of DNA extending from the tip of the X chromosome of Drosophila melanogaster. Within this sequence, we predict 277 protein coding genes, of which 94 had been sequenced already in the course of studying the biology of their gene products, and examples of 12 different transposable elements. We show that an interval between bands 3A2 and 3C2, believed in the 1970s to show a correlation between the number of bands on the polytene chromosomes and the 20 genes identified by conventional genetics, is predicted to contain 45 genes from its DNA sequence. We have determined the insertion sites of P-elements from 111 mutant lines, about half of which are in a position likely to affect the expression of novel predicted genes, thus representing a resource for subsequent functional genomic analysis. We compare the European Drosophila Genome Project sequence with the corresponding part of the independently assembled and annotated Joint Sequence determined through "shotgun" sequencing. Discounting differences in the distribution of known transposable elements between the strains sequenced in the two projects, we detected three major sequence differences, two of which are probably explained by errors in assembly; the origin of the third major difference is unclear. In addition there are eight sequence gaps within the Joint Sequence. At least six of these eight gaps are likely to be sites of transposable elements; the other two are complex. Of the 275 genes in common to both projects, 60% are identical within 1% of their predicted amino-acid sequence and 31% show minor differences such as in choice of translation initiation or termination codons; the remaining 9% show major differences in interpretation.

[All of the sequences analyzed in this paper have been deposited in the EMBL-Bank database under the following accession nos.: AL009146, AL009147, AL009171, AL009188-AL009196, AL021067, AL021086, AL021106-AL021108, AL021726, AL021728, AL022017, AL022018, AL022139, AL023873, AL023874, AL023893, AL024453, AL024455-AL024457, AL024485, AL030993, AL030994, AL031024-AL031028, AL031128, AL031173, AL031366, AL031367, AL031581-AL031583, AL031640, AL031765, AL031883, AL031884, AL034388, AL034544, AL035104, AL035105, AL035207, AL035245, AL035331, AL035632, AL049535, AL050231, AL050232, AL109630, AL121804, AL121806, AL132651, AL132792, AL132797, AL133503-AL133506, AL138678, AL138971, AL138972, and Z98269. A single file (FASTA format) of the 2.6-Mb contig is available from ftp://ftp.ebi.ac.uk/pub/databases/edgp/contigs/contig_1.fa.]


15 Present address: Department of Genetics, School of Medicine, Washington University, 4566 Scott Avenue,St. Louis, MO 63110 USA.

16 Corresponding author.


11:710-730 ©2001 by Cold Spring Harbor Laboratory Press  ISSN 1088-9051/01 $5.00

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